Tetracycline removal from wastewater via g-C3N4 loaded RSM-CCD-optimised hybrid photocatalytic membrane reactor

In this study, a split-type photocatalytic membrane reactor (PMR), incorporating suspended graphitic carbon nitride (g-C3N4) as photocatalyst and a layered polymeric composite (using polyamide, polyethersulfone and polysulfone polymers) as a membrane was fabricated to remove tetracycline (TC) from aqueous solutions as the world's second most used and discharged antibiotic in wastewater. The photocatalyst was synthesised from melamine by ultrasonic-assisted thermal polymerisation method and, along with the membrane, was characterised using various methods, including Brunauer–Emmett–Teller analysis (BET), Fourier-transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), Field emission scanning electron microscopy (FESEM), and Ultraviolet–visible spectroscopy (UV–Vis). The PMR process was optimised, using Design-Expert software for tetracycline removal in terms of UV irradiation time, pH, photocatalyst loading, tetracycline concentration, and membrane separation iteration. It was revealed that a membrane-integrated reactor as a sustainable system could effectively produce clean water by simultaneous removal of tetracycline and photocatalyst from aqueous solution. The maximum removal of 94.8% was obtained at the tetracycline concentration of 22.16 ppm, pH of 9.78 with 0.56 g/L of photocatalyst in the irradiation time of 113.77 min after six times of passing membrane. The PMR system showed reasonable reusability by about a 25.8% drop in TC removal efficiency after seven cycles at optimal conditions. The outcomes demonstrate the promising performance of the proposed PMR system in tetracycline removal from water and suggest that it can be scaled as an effective approach for a sustainable supply of antibiotic-free clean water.


Synthesis of g-C 3 N 4
For g-C 3 N 4 synthesis, melamine was initially subjected to direct furnace heating.In a pot, 5g of melamine was placed and securely sealed with thick aluminium foil.The furnace temperature was then gradually increased at 10 °C/min up to 520 °C and maintained constant for two h.The resulting yellowish mass (g-C 3 N 4 ) was grounded using a mortar.The sieved materials were immersed in DDW, ultrasonicated for 90 min in three stages (to prevent agglomeration, particle stability, and increase specific surface area), and oven-dried at 70 °C for 24 h, as also confirmed by 29 .The resulting g-C 3 N 4 were kept in a sealed container for characterisation and testing purposes.

Characterization techniques
Field Emission Scanning Electron Microscope (FE-SEM, MIRA3 TESCAN-XMU, Czech Republic) was utilised for morphological assessment of the synthesised g-C 3 N 4 and used membrane, at a beam energy level of 30.00 kV under high vacuum conditions.The porous structure of the used materials was analysed based on the Brunauer Emmett Teller (BET) method by the use of the Micromeritics apparatus (ASAP2020, USA).

Experimental testing and optimisation
The schematic diagram of the bespoke laboratory-scale slurry PMR system developed for this study is presented in Fig. 1 and Fig. S1.The membrane with a layered structure made of polyester, polysulfone, and polyamide was purchased from Sepanta Polymer Sharif Co. (Tehran, Iran).Table S1 presents the main properties of the commercial membrane.In each test, a predetermined amount of g-C 3 N 4 (0.2-1 g/L) was dispersed in a solution with specific pH and TC concentrations.Before being exposed to irradiation, the sample was magnetically stirred for 30min in a dark environment to establish an adsorption-desorption equilibrium.Photocatalytic degradation tests were carried out under visible light irradiation for a specific time (60-120min) using a 300W Xenon lamp (TACPRO, WLY202009) with a 420nm cut-off filter.The solution was centrifuged at 7500rpm for 8 min to take photocatalyst-free samples.A cylindrical module with a 5-bar retentate static N 2 pressure was used to perform the membrane separation process.The UV-Vis spectrophotometer was employed to detect TC concentration in the permeate solution at max = 356.5 nm and determine TC removal (%) using the following equation: where C 0 and C t are initial and final TC concentrations, respectively.
The response surface methodology (RSM), based on a central composite design (CCD), was used in this study for optimisation purposes, using design-expert software (Ver.12.0.3,USA).The main objective was to analyse the effects of intended independent parameters, develop regression models, and determine the optimal conditions for PMR-based removal of TC from water.The experimental designs were randomised, and mean values were used.The ranges for the independent factors determined based on the existing literature, preliminary tests, and material properties were as follows: irradiation time (60-120 min), initial pH level (7-13), catalyst concentration (0.2-1 g/L), initial TC concentration (10-30 mg/L), and filtration cycles (2-6 times).In total, 50 tests were carried out, and a summary of experimental conditions and their corresponding responses is provided in Table 1 for photocatalytic degradation and PMR removal.The relationship between the independent variables and responses was analysed via fitting a quadratic polynomial function.The significance and precision of the model were then evaluated through variance analysis (ANOVA), and the fitness of the model was expressed using the coefficients of determination (R 2 , R 2 adj, and R 2 pred ).

XRD and FTIR analysis
The g-C 3 N 4 nanosheets' XRD patterns are depicted in Fig. 2a.The peaks at 27.66° and 13° can be associated with the (002) and (100) crystal planes of the g-C 3 N 4 structure, respectively 30 .The sharp peak at 27.66° may indicate the interlayer distance of the g-C 3 N 4 nanosheets, also known as graphitic carbon nitride, which can be influenced by intercalation, doping, or modification of g-C 3 N 4 .The presence of the (100) crystal plane can confirm that the synthesised materials is in the form of nanoplates rather than bulk material 31 .The (100) plane corresponds to a parallel layer arrangement held together by weak van der Waals forces 32 .The obtained X-ray diffraction spectrum aligns with findings reported in other studies [33][34][35][36] .Figure 2b presents the FTIR spectrum of the synthesised g-C 3 N 4 materials.The wide peak at 3152 cm −1 can be related to the N-H stretching of s-triazine rings 37 , while, the peaks ranging 1628-1231 cm −1 are attributed to the stretching vibrations of the aromatic C-N heterocycle 38 .
The sharp peak at 804 cm −1 points to the presence of 3D heptazine structures within the g-C 3 N 4 nanosheets 33,38,39 .

FE-SEM, BET and zeta potential analysis
The morphology and nanostructured skeleton of the synthesised g-C 3 N 4 were studied through a FE-SEM analysis and presented in Fig. 3.The FESEM image can provide further evidence of the two-dimensional layered structure of g-C 3 N 4 , appearing as sheets with wrinkles.It can be attributed to the polycondensation of melamine molecules, leading to the formation of g-C 3 N 4 sheets.The nanostructures of g-C 3 N 4 tend to have a sheet-like appearance due to their graphite-like structure.Moreover, the FESEM image demonstrated the presence of a porous g-C3N4 structure, with numerous pores observed on the surface as well as within the nanostructure itself.
The porosity of the g-C 3 N 4 nanosheets was analysed using BET technique based on N 2 adsorption-desorption isotherm as shown in Fig. 4a and Table S2.The g-C 3 N 4 average pore size is less than 50 nm (9.04 nm), showing a mesoporous material according to the IUPAC classification.The specific surface area is 36.31m 2 /g, significantly higher than the reported values in the literature for pure g-C 3 N 4 : 8.56 m 2 /g 40 and 14.67 m 2 /g 41    www.nature.com/scientificreports/elevated specific surface area of the g-C 3 N 4 synthesised in this study may be related to the additional sonication step during the thermal polycondensation of melamine.The characteristic hysteresis isotherm of type IV in the P/P 0 range of 0.4-1.0 can indicate a uniform pore size distribution 37 .Zeta potential analysis was conducted at various pH levels at the room temperature to assess the surface charge and stability of g-C 3 N 4 (Fig. 4b).The synthesised photocatalyst showed a relatively low stability at higher pH levels, as evidenced by its low zeta potential, and the maximum stability can be seen at a pH of 10.It was also reported that the emulsion of the g-C 3 N 4 photocatalyst maintained its stability at neutral pH 42 .The detailed data of Zeta potential analysis can be found in Table S3 in the supplementary data.

Membrane characterisation
The membrane's porosity, pore size distribution, specific surface area, and total pore volume were determined using BET analysis and provided in Table S4.The membrane average pore diameter about 4.75 nm, placing it in the category of mesoporous materials 43 .Figure 4c displays N 2 adsorption-desorption isotherm for the membrane, corresponding to type VI of the IUPAC classification.The isotherm shows that the membrane is composed of multiple layers of different pore sizes 44 .According to Fig. 4d, most of the pores have a diameter between 2.4 to 5.4 nm.The number of pores with a size larger than 5.4 nm decreases drastically.The membrane morphology evaluated by FESEM can be seen in Fig. 5a-c showing the groove like pores of the membrane.
Figure 5e-h displays the cross-section images of the membrane.The membrane displayed a characteristic asymmetrical shape, with sponge-like structures in the intermediate layers of the membrane and a dense skin layer on the top and bottom.Furthermore, it was clear that each membrane exhibited a uniformly porous interior structure.The results of the analysis of the membrane's contact angle are shown in Fig. S3.Higher membrane hydrophilicity results from a lower contact angle.These were determined by measuring the contact angle of a www.nature.com/scientificreports/static water drop at 25 °C room temperature.The contact angle measurements showed that the membrane has a water contact angle of 0° (after three independent experiments), indicating the super hydrophilic property of this membrane.Figure 6a,b displays the membrane's 2 and 3D dimensional AFM images at scan sizes of 1.16 µm × 1.6µm.In order to precisely assess the roughness, Table S5 provides the mean distance (Rq) between peaks and valleys, the average roughness (Ra), and the difference (Rz) between high peaks and low valleys that were calculated from AFM analysis.The results, which show Ra = 16.23,Rq = 20.53, and Rz = 130.0 nm, imply that a smoother

Preliminary control testing
To assess the potential adsorption of TC on g-C 3 N 4 , the strategy of dark control test was followed.A 100 ml emulsion of 20 mg/L TC and 0.5 g/L g-C 3 N 4 was prepared in a beaker.The beaker was then tightly covered with thick aluminium foil to ensure a dark environment and kept undisturbed for 24 h.The initial pH of the sample was about 6.6.TC concentration in the sample was recorded using UV-Vis spectroscopy, and just 2.2% of TC was removed through dark adsorption which can be attributed to the limited electrostatic interaction between TC and g-C 3 N 4 at a pH of 6.6.The photocatalytic degradation of TC was tested with varying parameters of the irradiation time (60-120 min), initial pH (7-13), catalyst concentration (0.2-1 g/L), and initial TC concentration (10-30 mg/L).The reaction mixture was sampled, centrifuged, and analysed using UV-Vis spectroscopy as summarised in Table S6.The highest TC degradation of 63% was achieved in run number of 4, as determined by the Design-Expert software and based on the proposed operating conditions.The separability of the used membrane for TC was evaluated via 15 filtration cycles of 20 mg/L TC aqueous solution analysed by UV-Vis spectroscopy (Fig. S4 in supplementary information).The maximum TC removal achieved was 74.4%, mainly due to adsorption and size exclusion mechanisms.The molecular weight of TC is 480.9 g/mol, which is close to the membrane molecular weight cut-off (MWCO) of 400 Da can indirectly points to the size exclusion as a crucial role in removing TC from the aqueous solution 45,46 .www.nature.com/scientificreports/

PMR-based removal of TC
In this study, the performance of a split-type PMR in removal of TC from water was optimised using Design-Expert software based on CCD-based RSM optimization, in terms of five independent parameters of irradiation time, pH, catalyst dosage, TC initial concentration, and filtration iteration.This approach effectively minimises the number of experiments required, simplifies the identification of synergistic or antagonistic effects among factors, validates the obtained data, and quantifies the interactions between different factors.Based on the optimisation outcome, 50 tests were carried out and their results are tabulated in Tables S5.The maximum and minimum removal of TC using the split-type PMR were reported as 92% and 57%, respectively.

ANOVA analysis
The results of ANOVA analysis for removal of TC from water are provided in Table 1 and Table S7.Following PMR-based removal of TC, regression models were developed using CCD method to determine the relationship between removal efficiency and five independent variables.The variables, namely irradiation time, pH, catalyst dosage, TC initial concentration, and filtration cycles, were noted as A, B, C, D, and E, respectively, in the proposed equation (Eq.2).The equation includes a constant value, linear terms, and quadratic terms to show the individual effects of each parameter, as well as cross product terms to evaluate the interactive effects of parameters on the response.After removing insignificant terms, the regression model was obtained, and the results are presented in Table 1.In this model, positive and negative coefficients represent a synergistic and antagonistic effect between the variables, respectively.Table 1 can confirm that each parameter individually played a significant role in PMR-based TC removal.The interaction of pH with catalyst dosage, TC initial concentration, and filtration cycles showed significant effects on the model.The variance analysis in Table S7 demonstrates the suitability of the proposed models with the Model F-value of 205.52 which indicates its significance.However, the lack of model fit is not significant which indicates that the model is capable of calculating random errors for the experimental data 47 .The plots of Predicted-vs-actual, normal probability, residuals vs run number, and box-cox are shown in Fig. S5 of supplementary information.Actual values were determined experimentally and predicted values were provided by the RSM model (Fig. S5a).Predicted-vs-Actual plot indicates that the model is adequate, ensuring the acceptability of the predicted model since almost all the points in both the plots lie on or in the vicinity of the diagonal line.The normal probability distribution of residuals is shown in Fig. S5b which depicts a high degree of fitness due to a linear profile with a minimal error; hence, the errors are distributed normally.In this study, based on the ANOVA results for responses in Table S7, the obtained R 2 , R 2 adj , and R 2 pred values for the removal of TC by split-type PMR are 0.98, 0.98, and 0.96, respectively.This indicates the adequacy of the suggested quadratic model.As observed, the adequate precision of the model is 55.83.The adequate precision measures the signal to noise ratio.A signal to noise ratio larger than 4 indicates that the model is able to navigate the design space 48 .

Effect of irradiation time and pH
Increasing the irradiation time initially enhanced TC removal due to the presence of empty active sites (Fig. 7a).However, as the irradiation duration increases and the active sites of the photocatalyst are being occupied, the impact of irradiation time diminishes 49,50 .The irradiation time has an optimal value, after which TC removal does not change.The maximum TC removal of 88.5% was achieved after 113.77 min at pH of 10, photocatalyst dosage of 0.6 g/L, TC initial concentration of 20 ppm, and 4 passes through the membrane.The impact of pH on TC removal using PMRs, as depicted in Fig. 7b, illustrates that TC removal initially increases with pH level, reaching its peak at 9.78.However, beyond that point, TC removal starts to decline with further increase in pH.The instability in photocatalyst reaction may be attributed to the change in surface electric charge of g-C 3 N 4 nanosheets at varied pH level as also observed by Zeta potential analysis.g-C 3 N 4 nanosheets had a negative electric charge over the pH range of 7-13, and particularly, at pH 10-13, it is lower in comparison to pH of 7-10.It is worth noting that, in the photocatalysis process, hydroxyl radicals play a crucial role 51 .At a higher pH, there are more hydroxide ions available within the solution, leading to increased production of hydroxyl radicals in the environment.However, as the pH continues to rise, hydroxide ions begin competing with TC molecules to occupy the photocatalyst active sites which negatively affects the photocatalytic removal of TC from aqueous solutions 52 .Overall, the maximum TC removal of 87% was achieved at specific operating conditions: pH level of 9.78, irradiation time of 90 min, photocatalyst dosage of 0.6 g/L, TC initial concentration of 20 ppm, and after 4 filtration cycles.As seen in Fig. 6a, the degradation efficiency of TC increases as the irradiation time increases from 60 to 105 min due to the enhanced interactions between TC and the photocatalyst, leading to the attack of hydroxyl radicals on TC and consequently degradation increase.However, when the irradiation time increased to 110min, degradation efficiency remains constant.This is likely due to the decrease in the number of active sites available for photocatalytic interactions.Beyond 110min, the degradation efficiency decreases as all available active sites become saturated, leading to no further increase and negative effect on degradation efficiency.

Effect of catalyst dosage
Figure 7c presents the impact of catalyst dosage on the PMR-based removal of TC.In essence, augmenting the photocatalyst concentration can enhance surface area availability for photon absorption, thereby accelerating oxidation reactions 53 .However, a higher chemical density of photocatalyst in the reactor can also lead to the www.nature.com/scientificreports/development of a turbid suspension, diminishing its transparency and photo penetration depth 54 .Furthermore, adding photocatalyst in a turbid suspension may result in photocatalyst aggregation and limit photocatalyst activities.Consequently, initially, raising the photocatalyst concentration linearly elevates photocatalytic removal rate; however, surpassing the optimal concentration of photocatalyst may not only fail to further increase TC removal but actually diminish it 55 .It is evident that the optimal photocatalyst loading should be determined as a very crucial parameter controlling photocatalyst activities from operational and economic viewpoints.The maximum TC removal of 87.5% was recorded at the photocatalyst dosage of 0.56 g/L, irradiation time of 90 min, pH of 10, TC initial concentration of 20ppm, and after 4 filtration iterations.This study discloses that increasing the amount of photocatalyst from 0.2 up to 0.6 g/L can effectively elevate the rate of degradation.However, at higher concentrations, beyond 0.6 g/L, light scattering can occur, reducing the transparency of the solution and decreasing photon access to the photocatalyst surface.Another reason for the efficiency reduction is the accumulation of catalysts in a clustered form, leading to a decrease in photon adsorption in the photocatalytic process.Therefore, the efficiency of photocatalytic degradation decreases with an increase in the amount of photocatalyst (> 6 g/L).

Effect of TC initial concentration
Figure 7d showcases the effects of pollutant initial concentration on the overall performance of PMR system.Within a certain range, elevating the pollutant primary concentration enhances the collision rate and oxidation reaction, leading to a better degradation up to an optimal dosage after which a relatively lower degradation rate is probable 22 due to increased emulsion turbidity and limited light absorbency.TC molecules at high concentrations may occupy the active sites of the photocatalyst, exerting a negative influence on the photocatalytic degradation process 13,56 .The maximum removal of TC (88.5%) was recorded at a TC concentration of 22.16 ppm, with an irradiation time of 90 min, pH of 10, photocatalyst dosage of 0.6 g/L, and after four membrane filtration cycles.
As the initial concentration of TC increases, the electron-hole pair ratio decreases, and active sites on the surface of the photocatalyst become saturated by TC molecules.This leads to less light entering the photocatalytic degradation system, and the efficiency of TC photocatalytic degradation decreases.Another reason may be the turbidity of the solution in which the photocatalytic reactions take place.The solution becomes cloudy, making www.nature.com/scientificreports/ it difficult for light to pass through, which reduces the amount of light irradiation on the photocatalyst surface and consequently reduces photocatalytic degradation efficiency.

Effect of membrane filtration cycle
Figure 7e provides some insight into the impact of membrane separation iterations on the TC removal using the developed PMR system.It is evident that more cycles of membrane filtration can result in higher amount of captured TC mainly due to size exclusion as evidenced based in the outcome of BET analysis.The maximum TC removal rate of 94.8% was achieved following an irradiation time of 90 min, at a pH level of 10, with a photocatalyst dosage of 0.6 g/L, an initial TC concentration of 20 ppm, and a total of six passes through the membrane.

Optimization of process operational parameters
The operating conditions yielding maximum PMR-based TC removal were determined based a CCD-based RSM optimisation carried out by Design-Expert software.The optimal range of parameters considered are provided in Table S8, leading to a set of conditions exhibiting greater desirability and feasibility (Table S9).To ensure accuracy, reliability, and reproducibility, the optimal points were experimentally tested three times.The results presented in Table S9 highlight a maximum degradation of 94.8%, closely aligning with the predicted software value of 96.2%.The concordance between the predicted and experimental outcomes underscores the model's reliability and its ability to accurately anticipate the maximum degradation of TC.Furthermore, the photocatalytic performance of TC photodegradation in this study has been systematically compared with pertinent literature Table 2.

Photocatalyst reusability and mechanism
The reusability of the synthesised photocatalyst in TC removal was analysed at optimal operating conditions (irradiation time of 113.77 min, pH level of 9.78, photocatalyst dosage of 0.56 g/L and TC concentration of 22.16 ppm) as an important marketability index as shown in Fig. 8.In brief, in each cycle, the used materials were recovered as follows.The photocatalyst was initially separated using centrifugation (at 7500 rpm for 7 min), then washed twice with 50 mL of ethanol (15 min magnetic stirring plus 6 min probe sonication at 100 watts), and followed by a complete DDW washing.The clean photocatalyst was oven-dried at 70 °C for 24 h.In order to investigate the economic justification of the g-C 3 N 4 photocatalyst for TC removal from aqueous solutions [70][71][72] .After seven cycles, the photocatalyst's TC removal efficiency, as shown in Fig. 8, reached 74.2%.It can be mainly attributed to two primary factors of blockage and degradation of active sites.The superficial active sites of the photocatalyst may become partially blocked by remaining TC molecules and reaction products, interrupting the photocatalytic interaction.Cyclic photocatalysis can also lead to the degradation or alteration of some active sites.Surface fouling, catalyst aging, and exposure to reactive species may also contribute to the active sites' deterioration, effectively diminishing their catalytic activities.These clues can highlight the importance of understanding the long-term challenges of photocatalysis.It also necessitates exploration of strategies for photocatalyst regeneration and optimisation to mitigate the decline in their removal efficiency 73 .The most crucial issue with fouling, degradation, or loss of photocatalytic activity over seven cycles is accumulation of TC molecules which may partially block the superficial active sites of the photocatalyst, impeding photocatalytic interactions.To mitigate the issues associated with the decline in photocatalyst efficiency after multiple cycles, it is required to improve the regeneration method to restore the photocatalyst's active sites after they have become partially blocked by TC molecules and reaction products over several cycles without causing significant damage or alteration to its structure.In addition, modification of the surface of the photocatalyst to make it less prone to blockage by TC    www.nature.com/scientificreports/It is also worth mentioning that the cost analysis, scaling viewpoints, and commercialisation aspects are all outside of the scope of this paper since the finalisation of scaling up/piloting is an imperative step before any valid cost analysis.However, cost analysis and feasibility study are recommended as topics for future research to pinpoint this technique.This study also does not discuss the environmental impact and sustainability issues of the photocatalyst and membrane used in the PMR system.It is crucial as topic for future research to assess the lifecycle impact of their synthesis, disposal, and potential release of harmful substances/by-products.Despite the promising performance, addressing these environmental impacts is vital in assessing the long-term sustainability of PMR technologies in practical settings.

Conclusions
This study investigated the degradation of tetracycline from water using a lab-scale photocatalytic membrane reactor (PMR) with a suspended graphitic carbon nitride (g-C3N4) photocatalyst and a layered polymeric polyester/polysulfone/polyamide membrane.A range of operating conditions were explored, and optimal parameters of irradiation time: 113.77min, pH: 9.78, photocatalyst dosage: 0.56g/L, tetracycline initial concentration: 22.16 mg/L, and 6 membrane passes resulted in a tetracycline removal efficiency of about 95%.The proposed hybrid approach, compared to individual photocatalysis and membrane processes, was confirmed to have about 32% and 20% higher removal efficiency, respectively.The designed PMR showed reasonable photocatalyst reusability, reaching 74% of maximum removal efficiency after seven cycles.Overall, the study's outcomes support the efficacy of the proposed PMR for tetracycline removal, offering a sustainable water treatment solution with a feasible hybrid photocatalyst-membrane process.

Figure 1 .
Figure 1.Schematic diagram of a laboratory scale split-type PMR with suspended photocatalyst.

Figure 4 .
Figure 4. (a) Nitrogen adsorption-desorption isotherms of g − C 3 N 4 , (b) Average values of g − C 3 N 4 zeta potential in aqueous suspensions at different pH, (c) nitrogen adsorption-desorption isotherms and (d) pore size distribution of the membrane.

Figure 5 .
Figure 5. (a-c) FESEM images of the surface and (d-h) FESEM cross-section images of the membrane of membrane.

Figure 6 .
Figure 6.(a,b) AFM images of Membrane, (c) particle size distribution histogram for membrane (average of particle size = 95.6 nm) and (d) histograms of roughness for membrane (pick to valley roughness = 130.0 nm).

Figure 7 .
Figure 7. Effect of (a) irradiation time, (b) pH, (c) catalyst dosage, (d) TC initial concentration, and (e) number of passes through membrane on TC removal from aqueous solutions.Fixed parameters, if applicable, were irradiation time = 90 min, pH = 10, photocatalyst dosage = 0.6 g/L, TC initial concentration = 20 ppm, number of passes through membrane = 4.

2 74 -
77 and h+74,78  , respectively, plays a key role in the g-C 3 N 4 photodegradation of TC.The potential g-C 3 N 4 for TC degradation pathways are shown in Fig.9based on the reactive species mentioned above.Upon irradiation of visible light on the g-C 3 N 4 photocatalyst, electrons and holes generate in the conduction and valence bands, respectively.As a result of the produced electrons and holes, TC is degraded down into CO 2 and H 2 O by reduction and oxidation processes with oxygen and water, respectively.

Figure 8 .
Figure 8. Photocatalyst removal efficiency in continuous cycles at optimum conditions.

Figure 9 .
Figure 9. Schematic diagram for the possible g-C 3 N 4 photodegradation mechanisms under visible-light irradiation.

Table 1 .
ANOVA results of quadratic model for TC Removal.

Table 2 .
Comparison of TC photocatalytic-degradation efficiency of this work with other visible-light-driven catalytic systems from recent literatures.
TC Con.